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Results of primary endoscopic Dacryocystorhinostomy surgery with and without silicon stenting in patients with epiphora

Comparing results of primary endoscopic Dacryocystorhinostomy (DCR) surgery with and without silicon stenting in patients with epiphora

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200718048126N1
Enrollment
72
Registered
2020-08-11
Start date
2020-08-22
Completion date
Unknown
Last updated
2024-08-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Primary acquired nasoLacrimal duct obstruction. Acquired stenosis of nasolacrimal duct

Interventions

Intervention 1: Intervention group: Patients undergoing endoscopic DCR surgery with stents placement. Intervention 2: Control group: Patients undergoing endoscopic DCR surgery without stents placemen

Sponsors

Rasht University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients 18 years of age and older with persistent epiphora or recurrent ocular discharge with primary diagnosis of acquired nasolacrimal duct obstruction referred to Amir Al-Momenin hospital of Rasht

Exclusion criteria

Exclusion criteria: Previous history of nasolacrimal duct surgery, suspicion of lacrimal sac malignancy, canalicular obstruction requires membranectomy, presence of punctum and eyelid ectropion and facial nerve palsy and lid lag, history of Radiotherapy and trauma and important disease in examined side of the nose and orbit, immunodeficiencies and uncontrolled systemic disease, congenital dacryocystitis, presence of abnormal bleeding disorder

Design outcomes

Primary

MeasureTime frame
Improvement of symptoms; nasolacrimal duct and ostium opening in endoscopy; No dacryocystitis. Timepoint: Patients will be followed up for 12 months. The first postoperative visit will take place in the first week and then in the 1st, 3rd, 6th and 12th months. All the consequences studies are examined in the all Visits. If patients have a stent, it will be removed during the third month visit. Method of measurement: The studied variables are examined by physical examination and nasal endoscopy in the first week after surgery and then 1st, 3rd, 6th and 12th months.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAkbari Maryam

Rasht University of Medical Sciences

M.akbari@gums.ac.ir0098 13 4139637459

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026